Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

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Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

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Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

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Item

label

Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

@en

Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

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Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

@en

Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

@nl

P1476

Genotypic and clinical heterogeneity within NCCN favorable-risk acute myeloid leukemia.

@en

P2093

Aaron C Shaver

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Adam C Seegmiller

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Cindy Vnencak-Jones

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Claudio A Mosse

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David R Head

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Michael Byrne

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P Brent Ferrell

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Robert D Daber

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Sanjay R Mohan

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Stephen A Strickland

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P2860

Prognostic Significance of KIT Mutations in Core-Binding Factor Acute Myeloid Leukemia: A Systematic Review and Meta-Analysis

CEBPA mutations in younger adults with acute myeloid leukemia and normal cytogenetics: prognostic relevance and analysis of cooperating mutations.

Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations.

Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype.

Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia (AML).

The impact of FLT3 internal tandem duplication mutant level, number, size, and interaction with NPM1 mutations in a large cohort of young adult patients with acute myeloid leukemia.

Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia.

RUNX1 mutations in acute myeloid leukemia: results from a comprehensive genetic and clinical analysis from the AML study group.

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia.

RUNX1 mutations are associated with poor outcome in younger and older patients with cytogenetically normal acute myeloid leukemia and with distinct gene and MicroRNA expression signatures.

P304

67-73

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P31

scholarly article

P356

10.1016/J.LEUKRES.2017.12.012

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P478

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P50

Michael Robert Savona

P577

2018-01-02T00:00:00Z

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P698

29310020

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P932

5856485

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